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American Journal of Medical Genetics. Part A|February 16, 2023
Expanding the reproductive organ phenotype of CHD7-spectrum disorderTomoki T Nomakuchi, Melinda Danowitz, Blythe Stewart, et al.
Journal of Autism and Developmental Disorders|February 21, 2019
A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early DevelopmentStuart K Shapira, Lin H Tian, Arthur S Aylsworth, et al.
The Journal of Thoracic and Cardiovascular Surgery|December 23, 2003
Apolipoprotein E genotype and neurodevelopmental sequelae of infant cardiac surgeryJ William Gaynor, Marsha Gerdes, Elaine H Zackai, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlationKaren W Gripp, Angela E Lin, Deborah L Stabley, et al.
Clinical Genetics|September 8, 2022
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expressionIan M Campbell, T Blaine Crowley, Chintan Jobaliya, et al.
Schizophrenia Research|July 16, 2018
Olfactory deficits and psychosis-spectrum symptoms in 22q11.2 deletion syndromeSunny X Tang, Paul J Moberg, James J Yi, et al.
Psychological Medicine|March 29, 2023
Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndromeRaquel E Gur, Donna M McDonald-McGinn, Tyler M Moore, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and managementAngela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.
Molecular Autism|November 2, 2017
Critical region within 22q11.2 linked to higher rate of autism spectrum disorderCaitlin C Clements, Tara L Wenger, Alisa R Zoltowski, et al.
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